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Yang, Changduk
Advanced Tech-Optoelectronic Materials Synthesis Lab.
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dc.citation.endPage 6567 -
dc.citation.number 17 -
dc.citation.startPage 6558 -
dc.citation.title CHEMISTRY OF MATERIALS -
dc.citation.volume 31 -
dc.contributor.author Qiu, Beibei -
dc.contributor.author Chen, Shanshan -
dc.contributor.author Li, Hongneng -
dc.contributor.author Luo, Zhenghui -
dc.contributor.author Yao, Jia -
dc.contributor.author Sun, Chenkai -
dc.contributor.author Li, Xiaojun -
dc.contributor.author Xue, Lingwei -
dc.contributor.author Zhang, Zhi-Guo -
dc.contributor.author Yang, Changduk -
dc.contributor.author Li, Yongfang -
dc.date.accessioned 2023-12-21T18:46:46Z -
dc.date.available 2023-12-21T18:46:46Z -
dc.date.created 2019-05-16 -
dc.date.issued 2019-09 -
dc.description.abstract Both photovoltaic performance and cost of materials are the key factors for commercial application of polymer solar cells (PSCs). In this study, we designed and synthesized two new conjugated polymers with a chlorine substituent at the α position and a flexible substituent on the β position of the thiophene conjugated side chain, J11 (with alkyl flexible substituent), and J12 (with alkoxy flexible substituent), through a relatively simple synthetic method. The two polymers displayed similar UV-vis absorption profiles with deep-lying HOMO (the highest occupied molecular orbital) energy levels. Compared with the alkyl substituted polymer J11, alkoxy substituted polymer J12 displayed slightly weaker aggregation and excessive miscibility with the n-type organic semiconductor (n-OS) m-ITTC (which is an isomeric counterpart of ITTC). As a result, the device based on J11:m-ITTC demonstrated a higher PCE of 12.32% with a high fill factor (FF) of 0.73, while the J12:m-ITTC-based device displayed a lower PCE of 8.74%, with a slightly higher V oc of 0.943 V but a low FF of 0.56, which should be ascribed to the relatively low hole mobility, resulting from its small phase separation. These results indicate that altering the position of the chlorine atom (Cl) from the β- to α-position of thiophene unit is a simple but effective method to prepare efficient chlorinated polymers for further development of PSCs. -
dc.identifier.bibliographicCitation CHEMISTRY OF MATERIALS, v.31, no.17, pp.6558 - 6567 -
dc.identifier.doi 10.1021/acs.chemmater.8b05352 -
dc.identifier.issn 0897-4756 -
dc.identifier.scopusid 2-s2.0-85064815845 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/27422 -
dc.identifier.url https://pubs.acs.org/doi/10.1021/acs.chemmater.8b05352 -
dc.identifier.wosid 000485830300023 -
dc.language 영어 -
dc.publisher American Chemical Society -
dc.title A Simple Approach to Prepare Chlorinated Polymer Donors with Low-Lying HOMO Level for High Performance Polymer Solar Cells -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Physical; Materials Science, Multidisciplinary -
dc.relation.journalResearchArea Chemistry; Materials Science -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus Phase separation -
dc.subject.keywordPlus Solar cells -
dc.subject.keywordPlus Solar power generation -
dc.subject.keywordPlus Thiophene -
dc.subject.keywordPlus Molecular orbitals -
dc.subject.keywordPlus Commercial applications -
dc.subject.keywordPlus High performance Polymer solar cells -
dc.subject.keywordPlus Highest occupied molecular orbital -
dc.subject.keywordPlus Low hole mobility -
dc.subject.keywordPlus Low-lying HOMO levels -
dc.subject.keywordPlus N-type organic semiconductor -
dc.subject.keywordPlus Photovoltaic performance -
dc.subject.keywordPlus UV-vis absorptions -
dc.subject.keywordPlus Polymer solar cells -
dc.subject.keywordPlus Conjugated polymers -
dc.subject.keywordPlus Electron energy levels -
dc.subject.keywordPlus Hole mobility -

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